Pteridine

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Pteridine
Skeletal formula of pteridine
Pteridine molecule
Pteridine molecule
Names
IUPAC name
pteridine
Identifiers
91-18-9 YesY
ChEBI CHEBI:27601 N
ChemSpider 1014 N
Jmol 3D model Interactive image
KEGG C07581 N
PubChem 1043
UNII 6EZF26XQ81 YesY
  • InChI=1S/C6H4N4/c1-2-9-6-5(8-1)3-7-4-10-6/h1-4H N
    Key: CPNGPNLZQNNVQM-UHFFFAOYSA-N N
  • InChI=1/C6H4N4/c1-2-9-6-5(8-1)3-7-4-10-6/h1-4H
    Key: CPNGPNLZQNNVQM-UHFFFAOYAU
  • C1=CN=C2C(=N1)C=NC=N2
Properties
C6H4N4
Molar mass 132.13 g·mol−1
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Pteridine is an aromatic chemical compound composed of fused pyrimidine and pyrazine rings. A pteridine is also a group of heterocyclic compounds containing a wide variety of substitutions on this structure. Pterins and flavins are classes of substituted pteridines that have important biological activity.

Pteridine is a precursor in the synthesis of dihydrofolic acid in many microorganisms. Pteridine and 4-aminobenzoic acid convert by the enzyme dihydropteroate synthetase into dihydrofolic acid in the presence of glutamate. The enzyme dihydropteroate synthetase is inhibited by sulfonamide antibiotics.

See also

References

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  • Voet, D.; Voet, J.G. (2004). Biochemistry (3rd ed.). John Wiley & Sons. ISBN 0-471-39223-5

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